Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotype (2017)
Source: American Journal of Medical Genetics - Part A. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, TRANSTORNOS DA ARTICULAÇÃO, DIAGNÓSTICO POR COMPUTADOR, SINAIS E SINTOMAS
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WADE, Emma M. et al. Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotype. American Journal of Medical Genetics - Part A, v. 173A, n. 7, p. 1739–1746, 2017Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.38267/epdf. Acesso em: 10 nov. 2024.APA
Wade, E. M., Jenkins, Z. A., Daniel, P. B., Morgan, T., Addor, M. C., Adés, L. C., et al. (2017). Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotype. American Journal of Medical Genetics - Part A, 173A( 7), 1739–1746. doi:10.1002/ajmg.a.38267NLM
Wade EM, Jenkins ZA, Daniel PB, Morgan T, Addor MC, Adés LC, Bertola D, Bohring A, Carter E, Cho T-J, Geus CM de, Duba H-C, Fletcher E, Hadzsiev K, Hennekam RCM, Kim CA, Deborah Krakow E, Morava E, Neuhann T, Sillence D, Superti-Furga A, Veenstra-Knol HE, Wieczorek D, Wilson LC, Markie DM, Robertson SP. Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotype [Internet]. American Journal of Medical Genetics - Part A. 2017 ; 173A( 7): 1739–1746.[citado 2024 nov. 10 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.38267/epdfVancouver
Wade EM, Jenkins ZA, Daniel PB, Morgan T, Addor MC, Adés LC, Bertola D, Bohring A, Carter E, Cho T-J, Geus CM de, Duba H-C, Fletcher E, Hadzsiev K, Hennekam RCM, Kim CA, Deborah Krakow E, Morava E, Neuhann T, Sillence D, Superti-Furga A, Veenstra-Knol HE, Wieczorek D, Wilson LC, Markie DM, Robertson SP. Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotype [Internet]. American Journal of Medical Genetics - Part A. 2017 ; 173A( 7): 1739–1746.[citado 2024 nov. 10 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.38267/epdf
